Publications by authors named "Ruo-gu Li"

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Dendritic cell mineralocorticoid receptor controls blood pressure by regulating T helper 17 differentiation: role of the Plcβ1/4-Stat5-NF-κB pathway.
Yong-Li Wang, Hong Zhu, Yi-Tong Pan, Da Shang, Lin-Juan Du, Wen-Zhen Lin, Yuan Liu, Yan Liu, Ruo-Gu Li

Eur Heart J· April 2025

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T-Cell Mineralocorticoid Receptor Deficiency Attenuates Pathologic Ventricular Remodelling After Myocardial Infarction.
Yong-Li Wang, Xiao-Xin Ma, Ruo-Gu Li, Hong Zhu, Lan Bai, Lin-Juan Du, Wen-Zhen Lin, Yuan Liu, Yan Liu

Can J Cardiol· May 2023

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An IL-6/STAT3/MR/FGF21 axis mediates heart-liver cross-talk after myocardial infarction.
Jian-Yong Sun, Lin-Juan Du, Xue-Rui Shi, Yu-Yao Zhang, Yuan Liu, Yong-Li Wang, Ting Liu, Yan Liu, Ruo-Gu Li

Sci Adv· April 2023

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NCOR1 maintains the homeostasis of vascular smooth muscle cells and protects against aortic aneurysm.
Lin-Juan Du, Jian-Yong Sun, Wu-Chang Zhang, Yuan Liu, Yan Liu, Wen-Zhen Lin, Ting Liu, Yong-Li Wang, Ruo-Gu Li

Cell Death Differ· March 2023

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Osteoblast MR deficiency protects against adverse ventricular remodeling after myocardial infarction.
Yong-Li Wang, Lan Bai, Xue-Rui Shi, Hong Zhu, Lin-Juan Du, Yuan Liu, Wen-Zhen Lin, Ting Liu, Yan Liu, Yu-Lin Li, Ruo-Gu Li

J Mol Cell Cardiol· June 2022

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Microbiota in Gut, Oral Cavity, and Mitral Valves Are Associated With Rheumatic Heart Disease.
Xue-Rui Shi, Bo-Yan Chen, Wen-Zhen Lin, Yu-Lin Li, Yong-Li Wang, Yan Liu, Ruo-Gu Li

Front Cell Infect Microbiol· July 2021

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Connexin45 (GJC1) loss-of-function mutation contributes to familial atrial fibrillation and conduction disease.
Ruo-Gu Li, Ying-Jia Xu, Willy G Ye, Yan-Jie Li, Honghong Chen, Donglin Bai

Heart Rhythm· May 2021

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Detection and functional characterization of a novel variation responsible for familial dilated cardiomyopathy.
Qi Qiao, Cui-Mei Zhao, Chen-Xi Yang, Jia-Ning Gu, Yu-Han Guo, Ruo-Gu Li

Clin Chem Lab Med· April 2021

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KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy.
Ning Li, Ying-Jia Xu, Hong-Yu Shi, Chen-Xi Yang, Yu-Han Guo, Ruo-Gu Li

Genes (Basel)· March 2021

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Nuclear receptor corepressor 1 represses cardiac hypertrophy.
Chao Li, Xue-Nan Sun, Bo-Yan Chen, Meng-Ru Zeng, Lin-Juan Du, Ting Liu, Yuan Liu, Yu-Lin Li, Yan Liu, Xu Liu, Ruo-Gu Li

EMBO Mol Med· November 2019

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HAND2 loss-of-function mutation causes familial dilated cardiomyopathy.
Hua Liu, Ying-Jia Xu, Ruo-Gu Li, Zhang-Sheng Wang, Min Zhang, Xiu-Mei Li

Eur J Med Genet· September 2019

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A New ISL1 Loss-of-Function Mutation Predisposes to Congenital Double Outlet Right Ventricle.
Zhi Wang, Hao-Ming Song, Fei Wang, Cui-Mei Zhao, Ri-Tai Huang, Ruo-Gu Li, Xing-Yuan Liu

Int Heart J· September 2019

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ISL1 loss-of-function mutation contributes to congenital heart defects.
Lan Ma, Juan Wang, Li Li, Qi Qiao, Ruo-Min Di, Xiu-Mei Li, Ruo-Gu Li, Xun Li

Heart Vessels· April 2019

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NR2F2 loss‑of‑function mutation is responsible for congenital bicuspid aortic valve.
Juan Wang, Pradhan Abhinav, Ying-Jia Xu, Ruo-Gu Li, Min Zhang, Xiu-Mei Li

Int J Mol Med· April 2019

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A loss-of-function mutation underlying familial atrial fibrillation.
Ning Li, Zhang-Sheng Wang, Xin-Hua Wang, Ying-Jia Xu, Qi Qiao, Xiu-Mei Li, Ruo-Gu Li

Int J Med Sci· February 2019

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ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy.
Yu-Min Sun, Jun Wang, Ying-Jia Xu, Xin-Hua Wang, Fang Yuan, Hua Liu, Ruo-Gu Li, Yan-Jie Li, Liang Zhao

Heart Vessels· July 2018

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A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect.
Xiao-Hui Qiao, Qian Wang, Juan Wang, Xing-Yuan Liu, Ying-Jia Xu, Yan-Jie Li, Ruo-Gu Li

Eur J Med Genet· April 2018

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TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus.
Ri-Tai Huang, Juan Wang, Song Xue, Xing-Biao Qiu, Hong-Yu Shi, Ruo-Gu Li, Hua Liu, Ning Li, Yan-Jie Li

Int J Med Sci· March 2018

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MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy.
Fang Yuan, Zhao-Hui Qiu, Xing-Hua Wang, Yu-Min Sun, Jun Wang, Ruo-Gu Li, Hua Liu, Liang Zhao, Xu Liu

Clin Chem Lab Med· February 2018

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GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve.
Ruo-Gu Li, Ying-Jia Xu, Juan Wang, Xing-Yuan Liu, Fang Yuan, Li Li, Hua Liu, Yan-Jie Li

Am J Cardiol· February 2018

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CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy.
Xing-Biao Qiu, Xin-Kai Qu, Ruo-Gu Li, Hua Liu, Ying-Jia Xu, Xu Liu

Clin Chem Lab Med· August 2017

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Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy.
Jia-Hong Xu, Jian-Yun Gu, Yu-Han Guo, Hong Zhang, Xing-Biao Qiu, Ruo-Gu Li, Hua Liu

Int Heart J· August 2017

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Impact of prior permanent pacemaker on long-term clinical outcomes of patients undergoing percutaneous coronary intervention.
Yan-Jie Li, Wei-Wei Zhang, Xiao-Xiao Yang, Ning Li, Xing-Biao Qiu, Ruo-Gu Li

Clin Cardiol· April 2017

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Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block.
Ying-Jia Xu, Xing-Biao Qiu, Fang Yuan, Hong-Yu Shi, Lei Xu, Xu Liu, Ruo-Gu Li

Mol Med Rep· April 2017

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CASZ1 loss-of-function mutation associated with congenital heart disease.
Ri-Tai Huang, Song Xue, Juan Wang, Jian-Yun Gu, Jia-Hong Xu, Yan-Jie Li, Ning Li, Hua Liu, Ruo-Gu Li

Gene· December 2016

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